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  4. N-Nitrosodiethylamine

N-Nitrosodiethylamine  (Synonyms: Diethylnitrosamine; DEN; DENA)

Cat. No.: HY-N7434 Purity: 99.98%
Handling Instructions Technical Support

N-Nitrosodiethylamine (Diethylnitrosamine) is a potent hepatocarcinogenic dialkylnitrosoamine. N-Nitrosodiethylamine is mainly present in tobacco smoke, water, cheddar cheese, cured, fried meals and many alcoholic beverages. N-Nitrosodiethylamine is responsible for the changes in the nuclear enzymes associated with DNA repair/replication. N-Nitrosodiethylamine results in various tumors in all animal species. The main target organs are the nasal cavity, trachea, lung, esophagus and liver.

For research use only. We do not sell to patients.

CAS No. : 55-18-5

Size Price Stock Quantity
Liquid + Solvent (Highly Recommended)
10 mM * 1 mL in DMSO
ready for reconstitution
In-stock
Solution
10 mM * 1 mL in DMSO In-stock
Liquid
500 mg In-stock
1 g In-stock
5 g In-stock
10 g   Get quote  
50 g   Get quote  

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This product is a controlled substance and not for sale in your territory.

Customer Review

Based on 6 publication(s) in Google Scholar

Other Forms of N-Nitrosodiethylamine:

Top Publications Citing Use of Products

    N-Nitrosodiethylamine purchased from MedChemExpress. Usage Cited in: Cancer Lett. 2025 Aug 10:217978.  [Abstract]

    N-Nitrosodiethylamine (DEN; 200 mg/kg; ip). The protein and mRNA levels of LGR5 were tested in tumor (T) and para-tumor (N) of DEN-induced hepatoma via western blot.

    N-Nitrosodiethylamine purchased from MedChemExpress. Usage Cited in: Cancer Lett. 2025 Aug 10:217978.  [Abstract]

    N-Nitrosodiethylamine (DEN; 200 mg/kg; ip). The protein and mRNA levels of LGR5 were tested in tumor (T) and para-tumor (N) of DEN-induced hepatoma via RT-qPCR.

    N-Nitrosodiethylamine purchased from MedChemExpress. Usage Cited in: Oncol Rep. 2023 Jul;50(1):142.  [Abstract]

    N-Nitrosodiethylamine (DEN; 40 mg/kg; ip). Histopathology of liver tissue from mice with DEN-induced primary liver cancer after LNT treatment. Histopathology of mouse liver tissues.

    N-Nitrosodiethylamine purchased from MedChemExpress. Usage Cited in: Oncol Rep. 2023 Jul;50(1):142.  [Abstract]

    N-Nitrosodiethylamine (DEN; 40 mg/kg; ip). Histopathology of liver tissue from mice with DEN-induced primary liver cancer. H&E staining of liver tissue sections from mice.

    N-Nitrosodiethylamine purchased from MedChemExpress. Usage Cited in: Oncol Rep. 2023 Jul;50(1):142.  [Abstract]

    N-Nitrosodiethylamine (DEN; 40 mg/kg; ip). Inhibitory effect of LNT on DEN-induced primary liver cancer in mice. The expression levels of EGR1, PTEN and other proteins in the liver tissues of the normal group and the model group, as analyzed by WB.

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    • Biological Activity

    • Purity & Documentation

    • References

    • Customer Review

    Description

    N-Nitrosodiethylamine (Diethylnitrosamine) is a potent hepatocarcinogenic dialkylnitrosoamine. N-Nitrosodiethylamine is mainly present in tobacco smoke, water, cheddar cheese, cured, fried meals and many alcoholic beverages. N-Nitrosodiethylamine is responsible for the changes in the nuclear enzymes associated with DNA repair/replication. N-Nitrosodiethylamine results in various tumors in all animal species. The main target organs are the nasal cavity, trachea, lung, esophagus and liver.

    In Vivo

    Note:
    Please do not refer to only one article to determine the experimental conditions. It is recommended to determine the optimal experimental conditions (animal strain, age, dosage, frequency and cycle, detection time and indicators, etc.) through preliminary experiments before the formal experiment.

    N-Nitrosodiethylamine can be used to create hepatocellular carcinoma models. In beagle dogs, after intravenous administration, the plasma concentration of N-Nitrosodiethylamine shows a biphasic decline, with an average distribution half-life of 19 minutes, an average elimination half-life of 73 minutes, an average total body clearance of 43.3 mL/min/kg, a steady-state distribution volume of 1.9 L/kg, and an average residence time of 45 minutes. The average bioavailability of the lowest oral dose reaches 93%[3].

    Induction of Liver Cancer[1][2]
    Background
    Cytochrome P450 enzyme activates nitrosamine metabolism as an active electrophilic agent, making it cytotoxic, mutagenic and carcinogenic[4].
    Specific Modeling Methods
    Male Wistar strain albino rats • 150-180 g • 12 weeks old
    Administration: 0.01% NDEA through drinking water for 15 weeks • or 200 mg/kg • i.p. • single dose
    Note
    (1)The liver tissues were examined histologically at 1-3 weeks after the administration of NDEA.
    (2)The rats were sacrificed by decapitation following overnight fast.
    Modeling Indicators
    Decreased final body weight and increased relative liver weight.
    Molecular changes: A decrease in the activities of SOD, CAT, GPx, GR, G6PD and GSH.

    MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

    Molecular Weight

    102.14

    Formula

    C4H10N2O

    CAS No.
    Appearance

    Liquid (Density: 0.95 g/cm3)

    Color

    Colorless to light yellow

    SMILES

    CCN(CC)N=O

    Structure Classification
    Initial Source
    Shipping

    Room temperature in continental US; may vary elsewhere.

    Storage

    4°C, protect from light

    *In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

    Solvent & Solubility
    In Vitro: 

    DMSO : 100 mg/mL (979.05 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

    H2O : 100 mg/mL (979.05 mM; Need ultrasonic)

    Preparing
    Stock Solutions
    Concentration Solvent Mass 1 mg 5 mg 10 mg
    1 mM 9.7905 mL 48.9524 mL 97.9048 mL
    5 mM 1.9581 mL 9.7905 mL 19.5810 mL
    View the Complete Stock Solution Preparation Table

    * Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
    Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (protect from light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

    * Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.

    • Molarity Calculator

    • Dilution Calculator

    Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

    Mass
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    Concentration
    ×
    Volume
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    Molecular Weight *

    Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

    This equation is commonly abbreviated as: C1V1 = C2V2

    Concentration (start)

    C1

    ×
    Volume (start)

    V1

    =
    Concentration (final)

    C2

    ×
    Volume (final)

    V2

    In Vivo:

    Select the appropriate dissolution method based on your experimental animal and administration route.

    For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
    To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for in vivo experiments, it is recommended to prepare freshly and use it on the same day.
    The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

    • Protocol 1

      Add each solvent one by one:  10% DMSO    40% PEG300    5% Tween-80    45% Saline

      Solubility: ≥ 2.5 mg/mL (24.48 mM); Clear solution

      This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).

      Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.

      Preparation of Saline: Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution.
    • Protocol 2

      Add each solvent one by one:  10% DMSO    90% (20% SBE-β-CD in Saline)

      Solubility: ≥ 2.5 mg/mL (24.48 mM); Clear solution

      This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).

      Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 900 μL 20% SBE-β-CD in Saline, and mix evenly.

      Preparation of 20% SBE-β-CD in Saline (4°C, storage for one week): 2 g SBE-β-CD powder is dissolved in 10 mL Saline, completely dissolve until clear.

    For the following dissolution methods, please prepare the working solution directly. It is recommended to prepare fresh solutions and use them promptly within a short period of time.
    The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

    • Protocol 1

      Add each solvent one by one:  PBS

      Solubility: 100 mg/mL (979.05 mM); Clear solution; Need ultrasonic and warming and heat to 60°C

    In Vivo Dissolution Calculator
    Please enter the basic information of animal experiments:

    Dosage

    mg/kg

    Animal weight
    (per animal)

    g

    Dosing volume
    (per animal)

    μL

    Number of animals

    Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
    Calculation results:
    Working solution concentration: mg/mL
    This product has good water solubility, please refer to the measured solubility data in water/PBS/Saline for details.
    The concentration of the stock solution you require exceeds the measured solubility. The following solution is for reference only.If necessary, please contact MedChemExpress (MCE).
    Purity & Documentation

    Purity: 99.98%

    References

    Complete Stock Solution Preparation Table

    * Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
    Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (protect from light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

    Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
    DMSO / H2O 1 mM 9.7905 mL 48.9524 mL 97.9048 mL 244.7621 mL
    5 mM 1.9581 mL 9.7905 mL 19.5810 mL 48.9524 mL
    10 mM 0.9790 mL 4.8952 mL 9.7905 mL 24.4762 mL
    15 mM 0.6527 mL 3.2635 mL 6.5270 mL 16.3175 mL
    20 mM 0.4895 mL 2.4476 mL 4.8952 mL 12.2381 mL
    25 mM 0.3916 mL 1.9581 mL 3.9162 mL 9.7905 mL
    30 mM 0.3263 mL 1.6317 mL 3.2635 mL 8.1587 mL
    40 mM 0.2448 mL 1.2238 mL 2.4476 mL 6.1191 mL
    50 mM 0.1958 mL 0.9790 mL 1.9581 mL 4.8952 mL
    60 mM 0.1632 mL 0.8159 mL 1.6317 mL 4.0794 mL
    80 mM 0.1224 mL 0.6119 mL 1.2238 mL 3.0595 mL
    100 mM 0.0979 mL 0.4895 mL 0.9790 mL 2.4476 mL

    * Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.

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      Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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    Product Name:
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